{"ok":true,"data":{"subject":{"kind":"trial","nctId":"NCT03948646","title":"Safety and Efficacy Study of Sofpironium Bromide in Subjects With Axillary Hyperhidrosis (BBI-4000-CL-302)","sponsor":"Botanix Pharmaceuticals","phases":["PHASE3"],"status":"COMPLETED","indication":null,"disease":"isolated familial wooly hair disorder"},"rows":[{"n":1,"question":"Is the biology right?","flags":[{"id":"somatic_driver","label":"Somatic driver evidence","value":"no","detail":"None of CHRM3, CHRM4, CHRM1 has somatic-mutation evidence in isolated familial wooly hair disorder","rule":"Open Targets has somatic-mutation evidence for the target in this cancer","source":{"label":"Open Targets: CHRM3 in isolated familial wooly hair disorder","url":"https://platform.opentargets.org/evidence/ENSG00000133019/MONDO_0008686","date":"2026-11-12T00:25:34.511Z"},"context":[]},{"id":"human_genetic","label":"Human genetic evidence","value":"no","detail":"No germline or somatic evidence for CHRM3, CHRM4, CHRM1 in isolated familial wooly hair disorder","rule":"Any germline or somatic human genetic evidence for the target in this cancer, counted apart from animal-model and literature evidence","source":{"label":"Open Targets: CHRM3 in isolated familial wooly hair disorder","url":"https://platform.opentargets.org/evidence/ENSG00000133019/MONDO_0008686","date":"2026-11-12T00:25:34.511Z"},"context":[]},{"id":"pediatric_target","label":"Pediatric target","value":"no","detail":"Not on the FDA list","rule":"Target is on FDA's Pediatric Molecular Target List (relevant targets); membership alone neither requires nor waives a study","source":{"label":"FDA Pediatric Molecular Target List (Listed as February 2026 on the FDA Pediatric Oncology page; the file served is 9.7.22_the_relevant_molecular_target_list.xlsx, whose Summary of Changes sheet is headed 'SEPTEMBER 2022 UPDATE' (footnote date 2022-09-01))","url":"https://www.fda.gov/media/191157/download?attachment","date":"2026-11-11T07:05:03Z"},"context":[]},{"id":"haematologic","label":"Haematologic cancer","value":"no","detail":"Solid tumour","rule":"From the indication, or the registry conditions when no indication matches","source":{"label":"ClinicalTrials.gov NCT03948646","url":"https://clinicaltrials.gov/study/NCT03948646","date":"2026-11-12T00:25:34.511Z"},"context":[{"figure":"Likelihood of approval from phase 1: 7.5% haematologic vs 4.6% solid","dataset":"BIO / Informa / QLS 2021","years":"2011–2020","caveat":"Population-level, not a prediction."}]}],"facts":[{"label":"CHRM3 (via Sofpironium Bromide)","text":"Open Targets has no association between CHRM3 and isolated familial wooly hair disorder.","source":{"label":"Open Targets: CHRM3 in isolated familial wooly hair disorder","url":"https://platform.opentargets.org/evidence/ENSG00000133019/MONDO_0008686","date":"2026-11-12T00:25:34.511Z"}},{"label":"CHRM4 (via Sofpironium Bromide)","text":"Open Targets has no association between CHRM4 and isolated familial wooly hair disorder.","source":{"label":"Open Targets: CHRM4 in isolated familial wooly hair disorder","url":"https://platform.opentargets.org/evidence/ENSG00000180720/MONDO_0008686","date":"2026-11-12T00:25:34.511Z"}},{"label":"CHRM1 (via Sofpironium Bromide)","text":"Open Targets has no association between CHRM1 and isolated familial wooly hair disorder.","source":{"label":"Open Targets: CHRM1 in isolated familial wooly hair disorder","url":"https://platform.opentargets.org/evidence/ENSG00000168539/MONDO_0008686","date":"2026-11-12T00:25:34.511Z"}}],"pending":[{"what":"Normal-tissue expression in vital organs","source":"Human Protein Atlas (ticket 36)"},{"what":"Pan-essential in cell lines","source":"DepMap (ticket 36)"},{"what":"Approved drug on this target","source":"Drugs@FDA (ticket 30)"}]},{"n":2,"question":"Can the result be trusted?","flags":[{"id":"randomised","label":"Randomised","value":"yes","detail":"Randomised allocation","rule":"Registry allocation field","source":{"label":"ClinicalTrials.gov NCT03948646","url":"https://clinicaltrials.gov/study/NCT03948646","date":"2026-11-12T00:25:34.511Z"},"context":[]},{"id":"small_denominator","label":"Small denominator","value":"no","detail":"351 enrolled; each patient moves a rate by 100 ÷ 351 = 0.3 points","rule":"Enrolment under 30; the arithmetic is shown, not a benchmark","source":{"label":"ClinicalTrials.gov NCT03948646","url":"https://clinicaltrials.gov/study/NCT03948646","date":"2026-11-12T00:25:34.511Z"},"context":[]},{"id":"primary_os","label":"Primary endpoint is overall survival","value":"no","detail":"Number of Participants (Vehicle Arm vs. Sofpironium Bromide Gel, 15%) With and Without an Observed ≥2-point Improveme…; Observed Change in Participant (Vehicle Arm vs SB Gel 15% Arm) Ranked Gravimetric Sweat Production From Baseline to E…","rule":"A registered primary outcome measure names overall survival","source":{"label":"ClinicalTrials.gov NCT03948646","url":"https://clinicaltrials.gov/study/NCT03948646","date":"2026-11-12T00:25:34.511Z"},"context":[{"figure":"Non-OS primary endpoint: odds ratio 2.79 for a positive phase 3","dataset":"Otsuka 2021, 400 phase 3 oncology trials","years":"to 2020","caveat":"Shown with the next figure: a surrogate is easier to hit, and often a weak guide to survival."},{"figure":"52% of surrogate-to-OS correlations are low","dataset":"Prasad 2015","years":"published to 2014","caveat":"Shown with the figure above."}]},{"id":"results_overdue","label":"Results overdue","value":"no","detail":"Results posted 2024-05-21","rule":"Primary completion (actual) more than 12 months ago and no results posted to the registry","source":{"label":"ClinicalTrials.gov NCT03948646","url":"https://clinicaltrials.gov/study/NCT03948646?tab=results","date":"2026-11-12T00:25:34.511Z"},"context":[]}],"facts":[],"pending":[{"what":"Treated and evaluable counts, assessor, confirmed response, follow-up and data cutoff","source":"Readout extraction (ticket 32)"},{"what":"Primary endpoint changed between registry versions","source":"Registry versions in the store (ticket 32)"}]},{"n":3,"question":"What must it beat?","flags":[],"facts":[],"pending":[{"what":"Control-arm result and approved therapies for the same segment, with label links","source":"Drugs@FDA, FDA labels and readouts (tickets 30, 32)"}]},{"n":4,"question":"Too crowded, or too late?","flags":[],"facts":[{"label":"Stopped on this target","text":"46 terminated, withdrawn or suspended trials of drugs against CHRM3; 5 give no reason. Reasons are quoted as the registry gives them on the target page.","source":{"label":"CHRM3: what already stopped","url":"/target/ENSG00000133019#stopped","date":"2026-11-12T00:25:34.530Z"}}],"pending":[{"what":"Programs on the target by phase and months behind the leader","source":"Programs and Drugs@FDA (ticket 33)"}]},{"n":5,"question":"Can it be approved, and stay approved?","flags":[{"id":"single_country","label":"Single-country","value":"yes","detail":"All 42 sites in United States","rule":"All listed sites are in one country; the share of US sites is shown","source":{"label":"ClinicalTrials.gov NCT03948646","url":"https://clinicaltrials.gov/study/NCT03948646?tab=locations","date":"2026-11-12T00:25:34.511Z"},"context":[]},{"id":"eu_pip","label":"EU paediatric investigation plan","value":"no","detail":"No EMA paediatric investigation plan decision names Sofpironium Bromide, 15%, Vehicle","rule":"An EMA PIP decision (agreement, modification or waiver) lists the drug as its active substance, exact name","source":{"label":"EMA data download (dated snapshot)","url":"https://www.ema.europa.eu/en/documents/report/medicines-output-paediatric_investigation_plans-output-json-report_en.json","date":"2026-11-11T09:12:26Z"},"context":[]},{"id":"eu_orphan","label":"EU orphan designation","value":"yes","detail":"EU/3/14/1343 withdrawn 15 Oct 2014: Treatment of pancreatic cancer; EU/3/22/2631 positive 21 Jun 2022: Prevention of retinopathy of prematurity; EU/3/17/1873 positive 22 May 2017: Treatment of paroxysmal nocturnal haemoglobinuria; EU/3/19/2201 positive 21 Aug 2019: Treatment of C3 glomerulopathy; +4 more","rule":"An EU orphan designation lists the drug as its active substance (exact name) or belongs to a medicine that does; withdrawn and expired designations are listed with their status","source":{"label":"EMA data download (dated snapshot)","url":"https://www.ema.europa.eu/en/documents/report/medicines-output-orphan_designations-json-report_en.json","date":"2026-11-11T09:12:26Z"},"context":[]},{"id":"eu_authorised","label":"Authorised in the EU","value":"no","detail":"EMA lists no centrally authorised medicine of Sofpironium Bromide, 15%, Vehicle","rule":"An EMA medicine record lists the drug as its active substance or INN, exact name; national-only authorisations are not in this file","source":{"label":"EMA data download (dated snapshot)","url":"https://www.ema.europa.eu/en/documents/report/medicines-output-medicines_json-report_en.json","date":"2026-11-11T09:12:26Z"},"context":[]},{"id":"fda_orphan","label":"FDA orphan designation","value":"not published","detail":"FDA's orphan designation database turns away automated requests, so this app does not read it; search it by hand at the link","rule":"Would be: an FDA orphan designation names the drug","source":{"label":"FDA orphan designations search","url":"https://www.accessdata.fda.gov/scripts/opdlisting/oopd/","date":""},"context":[]},{"id":"fda_ped_approval","label":"FDA pediatric oncology approval","value":"no","detail":"FDA's table lists no pediatric approval of Sofpironium Bromide, 15%, Vehicle","rule":"FDA's Pediatric Oncology Drug Approvals table names the drug","source":{"label":"FDA Pediatric Oncology Drug Approvals (content current as of 2026-03-03)","url":"https://www.fda.gov/about-fda/oncology-center-excellence/pediatric-oncology-drug-approvals","date":"2026-11-12T00:25:34.542Z"},"context":[]},{"id":"studies_under_18","label":"Registered studies open to children","value":"yes","detail":"6237 interventional studies of Sofpironium Bromide, 15%, Vehicle include patients under 18; 1210 are recruiting, not yet recruiting or active","rule":"The registry's age group includes Child (birth to 17 years), which also counts studies that set no minimum age","source":{"label":"ClinicalTrials.gov search","url":"https://clinicaltrials.gov/search?intr=%22Sofpironium+Bromide%22+OR+%2215%25%22+OR+%22Vehicle%22&aggFilters=ages%3Achild%2CstudyType%3Aint","date":"2026-11-12T00:25:34.557Z"},"context":[]}],"facts":[{"label":"Caveat","text":"Site counts are not patients per country, and trials registered only outside ClinicalTrials.gov are not covered. Where the sites are is a fact about the record, not a judgement of its quality."},{"label":"Rare pediatric disease voucher","text":"FDA, content current as of 29 Apr 2026: “As of February 3, 2026, enactment of the Consolidated Appropriations Act, 2026, the rare pediatric disease PRV program will sunset after September 30, 2029. FDA may not award any PRVs under this program after September 30, 2029.” Voucher sale prices are not shown here; they appear only as company-reported news.","source":{"label":"FDA: Rare Pediatric Disease Designation and Priority Review Voucher Programs","url":"https://www.fda.gov/industry/medical-products-rare-diseases-and-conditions/rare-pediatric-disease-designation-and-priority-review-voucher-programs","date":"2026-11-11"}}],"pending":[{"what":"Precedent approvals for target, modality and endpoint; accelerated-approval status","source":"Drugs@FDA and FDA accelerated-approval tables (ticket 30)"}]},{"n":6,"question":"Can the sponsor finish?","flags":[],"facts":[{"label":"Sponsor","text":"Botanix Pharmaceuticals (industry)","source":{"label":"ClinicalTrials.gov NCT03948646","url":"https://clinicaltrials.gov/study/NCT03948646","date":"2026-11-12T00:25:34.511Z"}},{"label":"study director","text":"Patricia Walker, MD PhD, Botanix Pharmaceuticals","source":{"label":"Person page","url":"/person/Patricia%20Walker%2C%20MD%20PhD","date":"2026-11-12T00:25:34.511Z"}}],"pending":[{"what":"Filed cash, quarterly spend and the runway arithmetic","source":"SEC XBRL company facts (ticket 37)"},{"what":"Sponsor's completed vs stopped oncology trials and results-reporting record","source":"Registry, by company (ticket 37)"}]}],"limits":"Public records cannot show: sales forecasts; a probability of success for this asset; full deal terms and net prices; FDA designations and action dates before approval (shown only as company-reported); clinical holds unless the company disclosed them; manufacturing; patents on unapproved drugs; whether preclinical findings have been replicated.","sources":[{"label":"ClinicalTrials.gov NCT03948646","url":"https://clinicaltrials.gov/study/NCT03948646","date":"2026-11-12T00:25:34.511Z"},{"label":"Open Targets Platform","url":"https://platform.opentargets.org","date":"2026-11-12T00:25:34.511Z"},{"label":"FDA Pediatric Molecular Target List (Listed as February 2026 on the FDA Pediatric Oncology page; the file served is 9.7.22_the_relevant_molecular_target_list.xlsx, whose Summary of Changes sheet is headed 'SEPTEMBER 2022 UPDATE' (footnote date 2022-09-01))","url":"https://www.fda.gov/media/191157/download?attachment","date":"2026-11-11T07:05:03Z"}]},"source":"ClinicalTrials.gov + Open Targets","fetchedAt":"2026-11-12T00:25:34.509Z"}